Medical Device Jobs in Limerick

Cook Ireland Ltd - Limerick
Overview The Regulatory Affairs Specialist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices 12000.0
from: irishjobs.ie - 9 days ago

Cook Ireland Ltd - Limerick
Code of conduct is considered in all business matters carried out on Cook's behalf. Qualifications Experience in a manufacturing environment/QC inspection role. Previous experience in medical devices 12000.0
from: irishjobs.ie - 2 days ago
Hollister Incorporated - F26 F3X5 Ballina, MY, IE
leadership, preferably in the medical device industry. Plant experience in a Quality management role required. Corporate experience in a senior management leadership role with domestic/international plant
from: Hollister Incorporated - 10 days ago

Cook Ireland Ltd - Limerick
with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets and providing regulatory affairs input for the functional areas. Reporting to: Principal Regulatory 12000.0
from: irishjobs.ie - 10 days ago

Cook Ireland Ltd - Limerick
Overview This role will lead a team of engineers focused on research, development, and implementation of new medical device designs. This role will be responsible for technical leadership within 12000.0
from: irishjobs.ie - 11 days ago
Hollister Incorporated - F26 F3X5 Ballina, MY, IE
Management experience preferred Length of Experience 8+ years of relevant industry experience preferably in medical devices Specialized skills / Technical knowledge Innovative/Creative Thinker – must
from: Hollister Incorporated - 22 days ago

Cook Ireland Ltd - Limerick
the pharmaceutical or medical device industry. Excellent organisational skills are required for this role. A minimum of 5 years analytical laboratory experience. Proven People management, problem solving 12000.0
from: irishjobs.ie - 9 days ago

Cook Ireland Ltd - Limerick
to date knowledge of medical device regulations, guidance and requirements relevant to Quality Assurance. Organise and manage site preparation and manage audit back rooms for Regulatory and Corporate Audits 12000.0
from: irishjobs.ie - 14 days ago
Hollister Incorporated - F26 F3X5 Ballina, MY, IE
to apply understanding, of medical device regulations. This includes but is not limited to: US: 21 CFR Part 820 Canada: Medical Device Regulations SOR/98-282 EU: Medical Device Directive 93/42/EEC
from: Hollister Incorporated - 14 days ago

Cook Ireland Ltd - Limerick
of relevant ISO, EU, FDA medical devices standards regulations is required. High self-motivation, self-starter with a passion for excellence. Good working knowledge of Microsoft Office. Willingness 12000.0
from: irishjobs.ie - 11 days ago